Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34886500
rs34886500
CDKN2A
CUI: C2314896
Disease: Familial Atypical Mole Melanoma Syndrome
Familial Atypical Mole Melanoma Syndrome 		0.010 GeneticVariation BEFREE In one family where the proband had a P48L mutation in CDKN2A exon 1, the DNS phenotype was studied in detail. 10338331

1999